Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer Joint Practice Guideline
出版年份 2011 全文链接
标题
Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer Joint Practice Guideline
作者
关键词
-
出版物
Journal of Genetic Counseling
Volume 21, Issue 4, Pages 484-493
出版商
Springer Nature
发表日期
2011-12-14
DOI
10.1007/s10897-011-9465-7
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Point: Justification for Lynch Syndrome Screening Among All Patients With Newly Diagnosed Colorectal Cancer
- (2017) Heather Hampel Journal of the National Comprehensive Cancer Network
- Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer
- (2013) Uri Ladabaum et al. ANNALS OF INTERNAL MEDICINE
- Dominantly Inherited Constitutional Epigenetic Silencing of MLH1 in a Cancer-Affected Family Is Linked to a Single Nucleotide Variant within the 5′UTR
- (2011) Megan P. Hitchins et al. CANCER CELL
- Recurrence and variability of germline EPCAM deletions in Lynch syndrome
- (2011) Roland P. Kuiper et al. HUMAN MUTATION
- Neoadjuvant Therapy Induces Loss of MSH6 Expression in Colorectal Carcinoma
- (2010) Fei Bao et al. AMERICAN JOURNAL OF SURGICAL PATHOLOGY
- The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer
- (2010) Mercy Mvundura et al. GENETICS IN MEDICINE
- Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review
- (2010) Scott M. Weissman et al. Journal of Genetic Counseling
- Selection of Endometrial Carcinomas for DNA Mismatch Repair Protein Immunohistochemistry Using Patient Age and Tumor Morphology Enhances Detection of Mismatch Repair Abnormalities
- (2009) Karuna Garg et al. AMERICAN JOURNAL OF SURGICAL PATHOLOGY
- Immunohistochemistry as First-line Screening for Detecting Colorectal Cancer Patients at Risk for Hereditary Nonpolyposis Colorectal Cancer Syndrome
- (2009) Jinru Shia et al. AMERICAN JOURNAL OF SURGICAL PATHOLOGY
- Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations
- (2009) E Barrow et al. CLINICAL GENETICS
- Calculation of Risk of Colorectal and Endometrial Cancer Among Patients With Lynch Syndrome
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- Risk and Epidemiological Time Trends of Gastric Cancer in Lynch Syndrome Carriers in The Netherlands
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- Germline hypermethylation ofMLH1andEPCAMdeletions are a frequent cause of Lynch syndrome
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- PMS2 involvement in patients suspected of Lynch syndrome
- (2009) Renée C. Niessen et al. GENES CHROMOSOMES & CANCER
- Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives
- (2009) GENETICS IN MEDICINE
- EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome
- (2009) Glenn E Palomaki et al. GENETICS IN MEDICINE
- Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer
- (2009) Floor J. Backes et al. GYNECOLOGIC ONCOLOGY
- Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer
- (2009) M P Hitchins et al. JOURNAL OF MEDICAL GENETICS
- Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers
- (2009) Laura Baglietto et al. JNCI-Journal of the National Cancer Institute
- Familial Colorectal Cancer Type X: The Other Half of Hereditary Nonpolyposis Colon Cancer Syndrome
- (2009) Noralane M. Lindor Surgical Oncology Clinics of North America
- The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations
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- Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?
- (2008) Katharina Wimmer et al. HUMAN GENETICS
- Accurate classification ofMLH1/MSH2missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR)
- (2008) Elizabeth C. Chao et al. HUMAN MUTATION
- The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome
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- Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer
- (2008) Heather Hampel et al. JOURNAL OF CLINICAL ONCOLOGY
- Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
- (2008) Marjolijn J L Ligtenberg et al. NATURE GENETICS
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